G-quadruplex compounds and cis-platin act synergistically to inhibit cancer cell growth in vitro and in vivo

被引:33
作者
Gunaratnam, Mekala [1 ]
Green, Colin [2 ]
Moreira, Joao Bruno [1 ]
Moorhouse, Adam D. [1 ]
Kelland, Lloyd R. [2 ]
Moses, John E. [1 ]
Neidle, Stephen [1 ]
机构
[1] Univ London, Sch Pharm, CRUK Biomol Struct Grp, London WC1N 1AX, England
[2] BioPark Hertfordshire, Antisoma Res Labs, Welwyn Garden City AL7 3AX, Herts, England
基金
英国工程与自然科学研究理事会;
关键词
G-quadruplex; Ligand; Telomere; Cis-platin; Synergy; HUMAN TUMOR-CELLS; TELOMERASE INHIBITOR; LIGAND RHPS4; ANTITUMOR-ACTIVITY; CYTOTOXIC AGENTS; BREAST-CANCER; DNA; METHOSULFATE; CONSISTENT; MECHANISM;
D O I
10.1016/j.bcp.2009.03.018
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The ability of two structurally diverse telomeric G-quadruplex-binding compounds to synergise the action of cis-platin has been investigated in two cancer cell lines. One compound is a trisubstituted acridine compound AS1410, a close analogue of BRACO-19, and the other is a non-polycyclic compound synthesised using click chemistry and containing two triazole rings. Both compounds produce growth arrest at sub-cytotoxic concentrations in the two cell lines (MCF7 and A549), with behaviour consistent with telomere targeting mechanisms. Synergistic behaviour was observed in both cell lines with both compounds in combination with cis-platin, but only when the ratio of AS1410:cis-platin is >1. In vivo turnout xenograft studies with the A549 lung cancer model and the trisubstituted acridine compound AS1410 showed only a modest anti-tumour effect when administered alone, but produced rapid and highly significant decreases in turnout volume when administered in combination with cis-platin. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:115 / 122
页数:8
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